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  • 1980-1984  (10)
  • 1960-1964  (6)
  • Polymer and Materials Science  (14)
  • Elicitor  (2)
  • 1
    ISSN: 1432-2048
    Keywords: Chalcone synthase ; Colletotrichum ; Elicitor ; Phaseolus ; Phenylalanine ammonia-lyase ; Phytoalexin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In wounded cotyledons ofPhaseolus vulgaris L. the accumulation of the 5-hydroxy isoflavonoids kievitone and 2′-hydroxygenistein precedes the major increases in the levels of the 5-deoxy compounds phaseollin and coumestrol. Increased phytoalexin levels are preceded by transient increases in the extractable activities of L-phenylalanine ammonia-lyase (EC 4.3.1.5.), chalcone synthase and chalcone isomerase (EC 5.5.1.6.). Accumulation of phytoalexins, above wounded control levels, is observed following treatment of excised cotyledons or hypocotyls with crude or fractionated elicitor preparations heat-released from the cell walls ofColletotrichum lindemuthianum. Chalcone synthase levels are also induced in cotyledons, although crude elicitor and all fractions suppress L-phenylalanine ammonia-lyase activity in both tissues. Kievitone is the major phytoalexin induced in cotyledons, whereas in hypocotyls phaseollin predominates. Patterns of phytoalexin accumulation have been studied in response to varying concentrations of the crude and fractionated elicitor; 5-hydroxy isoflavonoid accumulation is highly dependent upon elicitor concentration, the dose-response curves for kievitone accumulation showing maxima at around 1 μg glucose equivalents per cotyledon, minima at 2–3 μg equivalents and increasing induction at higher concentrations. Similar patterns are observed for L-phenylalanine ammonia-lyase and chalcone synthase levels, although the overall extent of these changes is masked by the high wound response. Accumulation of 5-deoxy isoflavonoids above control levels requires high elicitor concentrations; no experimental conditions were found under which phaseollin accumulated to higher levels than kievitone in cotyledons during the first 48 h after elicitation.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2048
    Keywords: Cell suspension culture ; Chalcone isomerase ; Elicitor ; Enzyme induction ; Phaseolus (chalcone isomerase) ; Phytoalexin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Approximately fourfold increases in the extractable activity of the enzyme chalcone isomerase (CHI, EC 5.5.1.6) were observed within 24 h of treatment of cell suspension cultures of Phaseolus vulgaris with a crude elicitor preparation heatreleased from the cell walls of the bean pathogen Colletotrichum lindemuthianum. The induction of CHI activity was highly dependent upon elicitor concentration, with maximum induction occurring in two discrete concentration ranges. A basal half-life for CHI〉32 h in control cultures was determined by labelling with 2H from 2H2O followed by analysis of the equilibrium distribution of enzyme activity in CsCl density gradients. Comparative density labelling indicated that at both the lower and higher effective elicitor concentrations, the induced appearance of CHI activity was the result of an apparent initial activation of pre-existing enzyme followed by an increase in the rate of de-novo synthesis of the enzyme as compared with non-elicited controls. The increased appearance of the enzyme over the first 8 h in elicitor-treated cultures was inhibited by cycloheximide, cordycepin and actinomycin D. The results are discussed in relation to the mechanisms of co-ordinate enzyme induction operating in French-bean cell cultures exposed to fungal elicitors.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 4283-4294 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Acoustic and thermally stimulated current measurements are reported as a function of cure for dicyanodiamide cured epoxy resins. It is found that the acoustic propagation is dominated by the generation of voids and does not directly reflect the extent of cure. In contrast, the thermally stimulated data correlate well with conductivity data, the amplitude of the space charge peak decreasing with increasing degree of cure and the dipole peak shifting to high temperatures as predicted from DSC data. Both methods exhibit potential as NDT methods for cure in resins.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It was established that phenol-2,4-disulfonyl chloride and α-naphthol-2, 4-disulfonyl chloride introduce new intramolecular or tertiary bonds into lysozyme. The phenolic hydroxyl group seems to make the cross linking reagents soluble in aqueous media; it was established that a sulfonylating; species does dissolve prior to hydrolysis but that the chlorosulfonyl groups are hydrolyzed within seconds of dissolution. New covalently linked residues were shown to be introduced by different, spectra. Peptide maps of the lysozyme treated with phenol-2,4-disulfonyl chloride. peroxidized, and digested with trypsin showed definite deletions and additions when compared with the control. Partial analysis of the peptides showed that cross linking between ε-amino groups of lysine residues had occurred. A certain degree of stabilization of lysozyme to inactivation by certain inactivating conditions was noted after treatment with the two reagents. Ultra-centrifugal analysis of the lysozyme treated with phenol-2,4-disulfonyl chloride showed that there was no detectable fraction having a higher molecular weight than native lysozyme. Tentative assignments of positions of cross linking were made.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 23 (1984), S. 2671-2714 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A theory of polyelectrolyte effects on site-binding equilibria is generalized to multivalent ligands, multivalent supporting salt, intercalation, and multiple-site exclusion. The theory, which contains no adjustable parameters, except the number of sites excluded by a bound ligand, gives the dependence of the equilibrium constant on the binding fraction and the salt concentration. The theory is compared with prior experimental data for the dissociation of poly(acrylic acid), the binding of magnesium to polyphosphate, and the binding of ethidium and actionomycin D to DNA. The theory predicts the binding fraction dependence of the dissociation constant of poly(acrylic acid) well. The theory predicts the binding fraction dependence of the association constant of the binding of Mg2+ to polyphosphate well, if either one or two phosphates are bound by a magnesium ion. We conclude that polyelectrolyte effects on drug-DNA equilibria must be substantial. It follows that an incorrect estimate of the number of sites excluded by a bound drug molecule (because of its size or some other nonpolyelectrolyte effect) can be obtained from binding data if polyelectrolyte effects are ignored. The estimate is also within the context of, and subject to the validity of, the model used to describe the nonpolyelectrolyte contribution to binding. Our results suggest that, subject to these conditions, the anticooperativity of the binding of ethidium to DNA might be explained solely in terms of polyelectrolyte effects, and without reference to multiple-site exclusion, if sequence-specificity effects can be safely ignored. Our results also suggest that as few as two base pairs might be excluded by an actinomycin molecule. The theory gives fairly good agreement for the salt-concentration dependence of the association constant of all of the systems studied, including the complex of the neutral drug actinomycin with DNA.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 783-787 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Monomers of vinyl formate, vinyl acetate, vinyl propionate, and vinyl butyrate were carefully purified by distillation in a Vigreux column and in a 56-plate glass helixpacked Todd column. The refractive indices and boiling points of the purified monomers agreed with those given in the literature. The purified samples were exposed to the radiation of a quartz mercury lamp in order to produce several per cent polymer. The refractive indices are tabulated and plotted in graphs.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 1015-1022 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The steady-state (d.c.) electrical conductivity of polypropylene has been measured as a function of temperature (25-150°C.) and field strength (0-94 kv./cm.). The temperature coefficient of the conductivity is 34.6 kcal./mole expressed as an activation energy. This is much larger than the activation energy for diffusion of small molecules in the same polymer. Thus, ionization rather than diffusion appears to be the primary activation process. The conductivity is nonohmic; the conductance quotient is a linear function of field strength but is larger than predicted by Onsager's theory. The ion “jump distance” as evaluated from the isothermal field dependence, is the same order of magnitude as the diffusional mean free path estimated from diffusion studies in other polymers. The conductivity, conduction activation energy, and field dependence appear to be relatively insensitive to polymer crystallinity.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 2363-2379 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Dielectric measurements are reported on amine-cured epoxy resin samples over a frequency range from 200 Hz to 200 kHz and a temperature range from -60°C to 70°C as a function of molecular weight of the diglycidyl ether and water content. The effects of change of the molecular weight of the diglycidyl ether on the dielectric relaxation are small in comparison with the changes observed on the introduction of water into the matrix. Analysis of the data indicates the presence of cluster - free and bound - molecularly dispersed water. The former are presumed to be found in voids and cavities which arise in curing powder samples. The conductivity of the water-doped samples reflects the mobility of the water and is compared with the predictions of theories for amorphous materials.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 1329-1336 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of pentaerythritol (1) or dipentaerythritol with caprolactone yields prepolymers of the general structure \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm C} { \left( {\rm CH}_2 {\rm OH} \right)_4 } \hbox{--} {\rm i} \left [ {\rm CH}_2 {\rm O} \left( {\rm COCH}_2 {\rm CH}_2 {\rm CH}_2 {\rm CH}_2 {\rm CH}_2 {\rm O} \right)_{\rm n} {\rm H} \right]_{\rm i}$$\end{document} for i = 1, 2, 3, and 4 (2)-(5). The 13C chemical shifts of the quaternary carbons in (1)-(5) differ by more than 0.5 ppm. Conditions were determined to obtain quantitative intensity ratios of these carbons. The relative intensities give the distribution of the various branched structures and permit calculations of the average number of caprolactones per branch. Results are reported for caprolactone/polyol mole ratics of 3-66.
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 559-563 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C-NMR gives sequence information in copolyesters synthesized from ethylene glycol (EG), 1,4-butane diol (BD), and methyl terephthalate (TP). The EG-TP-EG and BD-TP-BD blocks are distinguishable from the unsymmetrical diester sequence EG-TP-BD. The carbonyl and aromatic quaternary carbons of terephthalate have different chemical shifts but identical relaxation times and nuclear Overhauser enhancements in the three different triad sequences. Peak areas indicate random copolymerization of the three copolyesters studied.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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